Unlocking the dual role of autophagy: A new strategy for treating lung cancer.

Journal of pharmaceutical analysis Pub Date : 2025-03-01 Epub Date: 2024-09-12 DOI:10.1016/j.jpha.2024.101098
Fei Tang, Jing-Nan Zhang, Xiao-Lan Zhao, Li-Yue Xu, Hui Ao, Cheng Peng
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Abstract

Lung cancer exhibits the highest incidence and mortality rates among cancers globally, with a five-year overall survival rate alarmingly below 20%. Targeting autophagy, though a controversial therapeutic strategy, is extensively employed in clinical practice. Current research is actively pursuing various therapeutic strategies using small molecules to exploit the dual function of autophagy. Nevertheless, the pivotal question of enhancing or inhibiting autophagy in cancer therapy merits further attention. This review aims to provide a comprehensive overview of the mechanisms of autophagy in lung cancer. It also explores recent advances in targeting cytotoxic autophagy and inhibiting protective autophagy with small molecules to induce cell death in lung cancer cells. Notably, most autophagy-targeting drugs, primarily natural small molecules, have demonstrated that activating cytotoxic autophagy effectively induces cell death in lung cancer, as opposed to inhibiting protective autophagy. These insights contribute to identifying druggable targets and drug candidates for potential autophagy-related lung cancer therapies, offering promising approaches to combat this disease.

揭示自噬的双重作用:治疗肺癌的新策略。
肺癌在全球癌症中发病率和死亡率最高,5年总生存率低于20%,令人震惊。靶向自噬虽然是一种有争议的治疗策略,但在临床实践中被广泛应用。目前的研究正在积极寻求利用小分子来开发自噬的双重功能的各种治疗策略。然而,增强或抑制自噬在癌症治疗中的关键问题值得进一步关注。本文综述了自噬在肺癌中的作用机制。探讨了靶向细胞毒性自噬和用小分子抑制保护性自噬诱导肺癌细胞死亡的最新进展。值得注意的是,大多数靶向自噬的药物,主要是天然小分子,已经证明激活细胞毒性自噬可以有效地诱导肺癌细胞死亡,而不是抑制保护性自噬。这些见解有助于确定潜在的自噬相关肺癌治疗的可药物靶点和候选药物,为对抗这种疾病提供了有希望的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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